Indications and uses
temporarily relieves these symptoms due to hay fever and other upper respiratory allergies: -runny nose -sneezing -itching of the nose and throat -itchy, watery eyes
temporarily relieves these symptoms due to hay fever and other upper respiratory allergies: -runny nose -sneezing -itching of the nose and throat -itchy, watery eyes
do not exceed recommended dose adults and children 12 years and over: take 1 tablet every 4 to 6 hours, as needed, not more than 6 tablets in 24 hours or as directed by a doctor children under 12 years: consult a doctor
Tamper Evident: Do not use if imprinted seal under cap is missing or broken. store at room temperature protect from moisture
Chlorpheniramine maleate 4 mg
Antihistamine
-runny nose
-sneezing
-itching of the nose and throat
-itchy, watery eyes
Ask a doctor before use if you have
• glaucoma
• trouble urinating due to an enlarged prostate gland
• a breathing problem such as emphysema or chronic bronchitis
Ask a doctor or pharmacist before use if youare taking sedatives or tranquilizers
When using this product
• drowsiness may occur
• avoid alcoholic drinks
• alcohol, sedatives and tranquilizers may increase drowsiness
• excitability may occur, especially in children
• use caution when driving a motor vehicle or operating machinery.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
cellulose, croscarmellose sodium, D and C yellow no. 10 lake, lactose, magnesium stearate, silica, stearic acid.
Product: 71335-1015
NDC: 71335-1015-1 30 TABLET in a BOTTLE
NDC: 71335-1015-2 60 TABLET in a BOTTLE
NDC: 71335-1015-3 100 TABLET in a BOTTLE
NDC: 71335-1015-4 120 TABLET in a BOTTLE
NDC: 71335-1015-5 40 TABLET in a BOTTLE
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-784-01 | EA - Each | 57896-784 | a1d38e1d-0a63-4d0c-b337-eb04a7b64e54 | 1 | 2014-04-03 |
| 57896-784-10 | EA - Each | 57896-784 | 5163bd9b-d641-4f83-87a1-c50108cd8e5e | 1 | 2018-06-11 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71335-1015 | 71335-1015-1, 71335-1015-2, 71335-1015-3, 71335-1015-4, 71335-1015-5 |
| 57896-784 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CHLORPHENIRAMINE MALEATE | V1Q0O9OJ9Z | ACTIB |
| ANHYDROUS LACTOSE | 3SY5LH9PMK | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| D&C YELLOW NO. 10 | 35SW5USQ3G | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 6d005729-843a-4726-a451-6824a3f41910 | b6afa521-55ea-455b-b43b-2f3c8469d60f | 2022-03-01 | Warnings | b6afa521-55ea-455b-b43b-2f3c8469d60f |
Adverse event summaries are temporarily unavailable. Other product information remains available.